Canonical Allele Identifier: CA2586964837

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475271del , CM000664.2:g.47475271del	GRCh38
NC_000002.11:g.47702410del , CM000664.1:g.47702410del	GRCh37
NC_000002.10:g.47555914del	NCBI36
NG_007110.2:g.77148del , LRG_218:g.77148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2005+1del
ENST00000233146.7:c.2005+1del
ENST00000543555.6:c.1807+1del
ENST00000644092.1:c.*305+1del
ENST00000645339.1:c.2005+1del
ENST00000645506.1:c.2005+1del
ENST00000646415.1:c.2005+1del
ENST00000233146.6:c.2005+1del
ENST00000406134.5:c.2005+1del
ENST00000543555.5:c.1807+1del
ENST00000610696.4:c.*401+1del
ENST00000613514.4:c.*545+1del
ENST00000617333.3:c.*771+1del
ENST00000617938.4:c.*977+1del
ENST00000621359.2:c.2005+1del
NM_000251.2:c.2005+1del , LRG_218t1:c.2005+1del
NM_001258281.1:c.1807+1del
XM_005264332.2:c.2005+1del
XM_011532867.1:c.2005+1del
XR_939685.1:n.2077+1del
XM_005264332.4:c.2005+1del
XM_011532867.2:c.2005+1del
XR_001738747.2:n.2067+1del
XR_939685.2:n.2067+1del
NM_000251.3:c.2005+1del